| Weight | 157.172 g/mol |
|---|---|
| Formula | C10H7NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Quinoline-6-carbaldehyde (4113-04-6)
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- Three novel transition metal complexes of 6-methyl-2-oxo-quinoline-3-carbaldehyde thiosemicarbazone: synthesis, crystal structure, cytotoxicity, and mechanism of action (RSC Advances, 2017)
- Angular group induced bond alternation (AGIBA). Part VIII. Crystal and molecular structure of 2,3,6,7-tetrahydro-1H, 5H-pyrido[3,2,1-ij]quinoline-9-carbaldehyde(E, E)-azine. A competition between the AGIBA and the through resonance effects (Polish Journal of Chemistry, 2002)
- Crystal structure of 11-oxo-2,3,6,7-tetrahydro-1H,5H,11H-pyrano[2,3-f]pyrido[3,2,1-ij]quinoline-10-carbaldehyde - a julolidine derivative, C16H15NO3 (Zeitschrift Fur Kristallographie-new Crystal Structures, 2017)
- Crystal structure and DFT study of 8-hydroxy-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline-9-carbaldehyde (Acta Crystallographica Section E: Crystallographic Communications, 2017)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=CC(=C2)C=O)N=C1
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InChIKeyVUAOIXANWIFYCU-UHFFFAOYSA-N
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